摘要
目的合成6-氨基苯并噻唑环类衍生物。方法以2-氨基-5-硝基苯硫醇为原料,通过环化、氨解、酰基化和硝基还原反应完成反应路线。结果合成了五个新型的6-氨基苯并噻唑环类衍生物,其结构经过1H-NMR表征。结论探索的反应路线方法可靠,操作简便。
Objective To synthesize 6-amino-benzothiazole ring derivatives. Methods With 2-amino-5-nitrothiophenol as raw material, synthetic strategy was completed by cyclization, ammonolysis, acylation and the reduction of nitro. Results Five novel 6-amino-henzethiazole ring derivatives were synthesized. The structures were characterized by 1H-NMR. Conclusions The method of the synthetic strategy is reliable and the operation
出处
《齐齐哈尔医学院学报》
2013年第12期1800-1801,共2页
Journal of Qiqihar Medical University
关键词
苯并噻唑环
衍生物
合成
Benzothiazole Ring
Derivatives
Synthesis